Q&A: SaMD Regulations and Compliant Development Environments Blog article written from the Q&A during the SaMD Regulations and Compliant Development Environments webinar. Various Authors - February 13, 2022 Blogs Medical Device Information Technology, Regulatory
Complaint Handling Integration with Salesforce Improves Patient Care Case study on Complaint Handling Integration with Salesforce Improves Patient Care. Jim Macdonell - February 12, 2022 Case Studies Medical Device Information Technology, Regulatory
The Origins of UDI Blog article topic: The Origins of UDI. Jay Crowley - February 11, 2022 Blogs Medical Device Manufacturing, Regulatory, Safety
GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Blog article topic: GCP Investigators: Do Regulations Require a CV to Be Updated Every Two Years? Diane Gleinser - February 10, 2022 Blogs Biotech, CMO, CRO, Medical Device, Pharma Quality Assurance, Regulatory
Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance On-demand webinar topic: Oracle Clinical One: Next Generation Clinical Trials with Continuous GxP Compliance. Webinars Biotech, CMO, CRO, Medical Device, Pharma Clinical, Information Technology, Regulatory
Onsite and Remote On-Demand Compliance Staff Augmentation Case study on Onsite and Remote On-Demand Compliance Staff Augmentation. Vega Finucan - February 6, 2022 Case Studies CMO, CRO Information Technology, Regulatory
